TBP, TATA-box binding protein, 6908

N. diseases: 158; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0497327
Disease: Dementia
Dementia
0.130 GeneticVariation disease BEFREE Finally, and with acknowledgement of the inadequacies of the literature to date, we advance a tentative classification of these disorders into three groups, based on the reported severity of their cognitive impairments, and correlated with their neuropathological topography and MRI findings: group 1-SCAs 6 and 8-mild dysexecutive syndrome based on disruption of cerebello-cortical circuitry; group 2-SCAs 1, 2, 3, and 7-more extensive deficits based largely on disruption of striatocortical in addition to cerebello-cerebral circuitry; and group 3-SCA 17 and DRPLA-in which cognitive impairment severe enough to cause a dementia syndrome is a frequent feature. 28708110 2017
CUI: C0497327
Disease: Dementia
Dementia
0.130 Biomarker disease BEFREE The SCA17 clinical phenotype includes characteristics associated with cerebellar and cortical atrophy such as ataxia, dementia, epilepsy, chorea and parkinsonian features. 21710129 2011
CUI: C0497327
Disease: Dementia
Dementia
0.130 GeneticVariation disease BEFREE This study demonstrates that CAG/CAA repeat expansion in the TBP gene causes ADCA with dementia and/or psychiatric manifestations. 11571212 2001
CUI: C0497327
Disease: Dementia
Dementia
0.130 Biomarker disease HPO